CD74 is a regulator of hematopoietic stem cell maintenance

被引:17
|
作者
Becker-Herman, Shirly [1 ]
Rozenberg, Milena [1 ]
Hillel-Karniel, Carmit [1 ]
Gil-Yarom, Naama [1 ]
Kramer, Mattias [1 ]
Barak, Avital [1 ]
Sever, Lital [1 ]
David, Keren [1 ]
Radomir, Lihi [1 ]
Lewinsky, Hadas [1 ]
Levi, Michal [1 ]
Friedlander, Gilgi [2 ,3 ]
Bucala, Richard [4 ]
Peled, Amnon [5 ]
Shachar, Idit [1 ]
机构
[1] Weizmann Inst Sci, Dept Immunol, Rehovot, Israel
[2] Weizmann Inst Sci, Ilana & Pascal Mantoux Inst Bioinformat, Rehovot, Israel
[3] Weizmann Inst Sci, Nancy & Stephen Grand Israel Natl Ctr Personalize, Rehovot, Israel
[4] Yale Sch Med, Internal Med, New Haven, CT USA
[5] Hadassah Hebrew Univ Hosp, Goldyne Savad Inst Gene Therapy, Jerusalem, Israel
关键词
D O I
10.1371/journal.pbio.3001121
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hematopoietic stem and progenitor cells (HSPCs) are a small population of undifferentiated cells that have the capacity for self-renewal and differentiate into all blood cell lineages. These cells are the most useful cells for clinical transplantations and for regenerative medicine. So far, it has not been possible to expand adult hematopoietic stem cells (HSCs) without losing their self-renewal properties. CD74 is a cell surface receptor for the cytokine macrophage migration inhibitory factor (MIF), and its mRNA is known to be expressed in HSCs. Here, we demonstrate that mice lacking CD74 exhibit an accumulation of HSCs in the bone marrow (BM) due to their increased potential to repopulate and compete for BM niches. Our results suggest that CD74 regulates the maintenance of the HSCs and CD18 expression. Its absence leads to induced survival of these cells and accumulation of quiescent and proliferating cells. Furthermore, in in vitro experiments, blocking of CD74 elevated the numbers of HSPCs. Thus, we suggest that blocking CD74 could lead to improved clinical insight into BM transplant protocols, enabling improved engraftment.
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页数:23
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